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Stargadt’s disease in two Nigerian siblings
Stargardt’s disease is an inherited macular dystrophy that is transmitted in an autosomal recessive or dominant pattern. The disorder is typically characterized by impairment of central vision, with onset around the first 10–20 years of life. Stargardt’s disease is rare in sub-Saharan Africa. This i...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove Medical Press
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3666157/ https://ncbi.nlm.nih.gov/pubmed/23750105 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/IMCRJ.S38683 |
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